Congenital Glucose-Galactose Malabsorption: A Case With a Novel SLC5A1 Mutation in a Saudi Infant

While only a few hundred cases have been reported in pediatrics, congenital glucose-galactose malabsorption (GGM) is an extremely rare autosomal-recessive metabolic disorder that is characterized by intractable diarrhea and severe dehydration, which can be life-threatening if not treated appropriate...

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Detalles Bibliográficos
Autores principales: Alamoudi, Loujen O, Alfaraidi, Albaraa T, Althagafi, Samiyah S, Al-Thaqafy, Majid S, Hasosah, Mohammed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8559579/
https://www.ncbi.nlm.nih.gov/pubmed/34737908
http://dx.doi.org/10.7759/cureus.18440

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8559579/
https://www.ncbi.nlm.nih.gov/pubmed/34737908
http://dx.doi.org/10.7759/cureus.18440

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